Canonical Allele Identifier: CA1158990186
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865598G= , CM000663.2:g.23865598G= GRCh38
NC_000001.10:g.24192088G= , CM000663.1:g.24192088G= GRCh37
NC_000001.9:g.24064675G= NCBI36
NG_013346.1:g.7772C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.417C= MANE Select ENSP00000363603.3:p.His139=
ENST00000374479.3:c.417C= ENSP00000363603.3:p.His139=
NM_000147.4:c.417C= NP_000138.2:p.His139=
XM_005245821.1:c.42C= XP_005245878.1:p.His14=
XM_011541167.1:c.-217C= XP_011539469.1:n.-217C=
XM_005245821.3:c.42C= XP_005245878.1:p.His14=
XM_011541167.3:c.-217C= XP_011539469.1:n.-217C=
XM_017000905.2:c.114C= XP_016856394.1:p.His38=
NM_000147.5:c.417C= MANE Select NP_000138.2:p.His139=
NR_174379.1:n.595C=
NR_174380.1:n.644C=
NR_174381.1:n.483C=
NR_174382.1:n.880C=